DUAL OPTIC, CURVATURE CHANGING ACCOMMODATIVE IOL

Description

FIELD

[0001] This present disclosure relates generally to the field of intraocular lenses (IOLs) and, more particularly, to accommodative IOLs.

BACKGROUND OF THE DISCLOSURE

[0002] The human eye in its simplest terms functions to provide vision by receiving light through a clear outer portion called the cornea, and focusing the image by way of a crystalline lens onto a retina. The quality of the focused image depends on many factors including the size and shape of the eye, and the transparency and focal power of the cornea and the lens.

[0003] When age or disease causes the lens to become less transparent, vision deteriorates because of the diminished amount of light that is transmitted to the retina. This deficiency in the lens of the eye is medically known as a cataract. An accepted treatment for this condition is surgical removal of the lens and replacement of the lens function by an artificial intraocular lens (IOL).

[0004] In the United States, the majority of cataractous lenses are removed by a surgical technique called phacoemulsification. During this procedure, an opening is made in the anterior capsule and a thin phacoemulsification cutting tip is inserted into the diseased lens and vibrated ultrasonically. The vibrating cutting tip liquefies or emulsifies the lens so that the lens may be aspirated out of the eye. The diseased lens, once removed, is replaced by an artificial lens.

[0005] In the natural lens, bifocality of distance and near vision is provided by a mechanism known as accommodation. The natural lens, early in life, is soft and contained within the capsular bag. The bag is suspended from the ciliary muscle by zonules. Relaxation of the ciliary muscle applies an axial force that tightens the zonules, and stretches the capsular bag. As a result, the natural lens tends to flatten. Tightening of the ciliary muscle relaxes the tension on the zonules, allowing the capsular bag and the natural lens to assume a more rounded shape. In this way, the natural lens can focus on both near and far objects.

[0006] As the lens ages, it becomes harder and is less able to change shape in response to movements of the ciliary muscle. This makes it harder for the lens to focus on near objects, a medical condition known as presbyopia. Presbyopia affects nearly all adults by the age of 45 or 50.

[0007] When a cataract or other disease requires the removal of the natural lens and replacement with an artificial IOL, the IOL typically is a monofocal lens that provides a suitable focal power for distance vision but requires the use a pair of spectacles or contact lenses for near vision. Multifocal IOLs, e.g., relying on diffractive patterns to general multiple foci, have been proposed but to date have not been widely accepted.

[0008] Therefore, a need exists for a safe and stable accommodative intraocular lens that provides accommodation over a broad and useful range.

[0009] Reference is made to US2012/0046744, US2005/0131535 and to US2009005865. US2009005865 describes a mechanism by which fluid is added to a chamber portion to change an optic power. US2005/0131535 relates to lenses including meniscus-shaped optics that include a chamber that is filled with gas (preferably air) and therefore is sealed from the surrounding environment. The power of the optic changes as the distance between the walls changes due to the chamber being sealed. US 2012/0046744 provides an IOL having a deformable membrane, and is considered representative of the state of the art. US 2012/0046744 does not disclose an arrangement in accordance with claim 1 in which the lens includes first and second membranes, a side wall connecting the membranes, and struts extending from the sidewall and coupling the fluid optic body to the second optic body.

SUMMARY OF THE DISCLOSURE

[0010] According to the invention there is provided an intraocular lens as defined in claim 1. Further optional features are provided in accordance with the dependent claims.

[0011] The present disclosure concerns curvature-changing, accommodative intraocular lenses (IOLs) that may be implanted in the capsular bag of a patient's eye and configured to harness the energy of the movement of the capsular bag upon contraction and relaxation of the ciliary muscles. In certain embodiments, the IOLs described herein are designed such that axial compression of the capsular bag changes the shape of a fluid optic (e.g., a fluid-filled cavity defined in part by a deformable optical membrane), thereby altering the curvature of the membrane and the power of the optic. As just one example, the IOLs described herein may include a fluid optic body and a second optic body each disposed on the optical axis and configured to be in contact with a surface of the capsular bag, the fluid optic body and the second optic body being coupled via a plurality of struts.

[0012] Upon axial compression of the capsular bag, an axial compressive force on the struts (e.g., via the second optical membrane) may cause the struts to deform (e.g., to pivot or to bow out), resulting in an increase in the tension on the deformable optical membrane (i.e., the deformable optical membrane may stretch radially). As a result, the curvature of the deformable optical membrane may be reduced, as in a disaccommodated native lens.

[0013] Conversely, when axial compression is relaxed, the deformation of the struts may be relieved and the deformable optical membrane may become more rounded to provide for close vision, as in an accommodated native lens. For example, the plurality of struts can be biased to rotate in a direction opposed to the first direction upon relaxation of the axial compression. In accordance with various aspects of the present teachings, the IOLs described herein can be implanted into the native capsular bag to replace a cataractous or presbyopic natural crystalline lens removed therefrom.

[0014] In certain embodiments, an IOL includes a fluid optic body having a cavity for containing an optical fluid, the cavity at least partially defined by a sidewall extending around the cavity and defining a diameter of the cavity and a deformable optical membrane intersecting the sidewall around a circumference of the sidewall and spanning the diameter of the cavity. The IOL further includes a second optic body spaced a distance apart from the fluid optic body and a plurality of struts extending from the sidewall and coupling the fluid optic body to the second optic body. The struts are configured such that axial compression of the capsular bag causes the plurality of struts to deform the sidewall in a manner that increases the diameter of the cavity such that a curvature of the deformable optical membrane is modified.

[0015] Certain embodiments of the present disclosure may provide an IOL that has a relatively small size and/or occupies a limited volume of the capsular bag while still providing a substantial power change between its accommodated and disaccommodated state. Accordingly, the presently disclosed IOL may allow for smaller surgical incisions during implantation. Additionally, the shape and/or stiffness of certain embodiments of the presently disclosed IOL may allow for interaction of the IOL with the capsule in a manner that prevents posterior capsule opacification (PCO) and anterior capsule opacification (ACO) via square edge optics, open capsule, and mechanical procedure.

BRIEF DESCRIPTION OF THE DRAWINGS

[0016] For a more complete understanding of the present disclosure and the advantages thereof, reference is now made to the following description taken in conjunction with the accompanying drawings in which like reference numerals indicate like features and wherein:

FIG. 1 is a perspective view of an exemplary curvature-changing, accommodative intraocular lens, according to certain embodiments of the present disclosure;

FIG. 2 is a cross-sectional view of the exemplary lens of FIG. 1;

FIG. 3A is a cross-sectional view of the exemplary lens of FIG. 1, depicting the lens in its accommodated (close vision) state within the capsular bag;

FIG. 3B is a cross-sectional view of the exemplary lens of FIG. 1, depicting the lens in its disaccommodated (near vision) state within the capsular bag;

FIG. 4A is a simulation of the pivoting of the struts and the curvature change of the deformable optical membrane of the exemplary lens of FIG. 1 as it moves from an accommodated state to a disaccommodated state;

FIG. 4B is another view of the simulation of the pivoting of the struts and the curvature change of the deformable optical membrane of the exemplary lens of FIG. 1 as it moves from an accommodated state to a disaccommodated state;

FIG. 5 is a perspective, cross-sectional view of another exemplary curvature-changing, accommodative intraocular lens, according to certain embodiments of the present disclosure;

FIG. 6 is a simulation of the movement of the exemplary lens of FIG. 6 as it moves from its resting or accommodated state to its disaccommodated state;

FIG. 7 is a plot depicting the power change of the exemplary lens of FIG. 6 as it moves from its resting or accommodated state to its disaccommodated state;

FIG. 8 depicts data showing the modulation transfer function and power change of the exemplary lens as shown in FIG. 1;

FIG. 9 is a cross-sectional view of another exemplary curvature-changing, accommodative intraocular lens, according to certain embodiments of the present disclosure;

FIG. 10 is a cross-sectional view of another exemplary curvature-changing, accommodative intraocular lens, according to certain embodiments of the present disclosure; and

FIG. 11 is a cross-sectional view of another exemplary curvature-changing, accommodative intraocular lens, according to certain embodiments of the present disclosure.

[0017] The skilled person in the art will understand that the drawings, described below, are for illustration purposes only. The drawings are not intended to limit the scope of the applicant's teachings in any way.

DETAILED DESCRIPTION

[0018] The present disclosure generally relates to an intraocular lens (IOL) configured to be implanted in the capsular bag of a patient and that can utilize the movement of the capsular bag to change the power of the IOL. With reference to FIGS. 1 and 2, an exemplary IOL 10 is depicted, according to certain embodiments of the present disclosure. As shown in FIG. 1, the IOL 10 generally comprises a fluid optic body 20 and a second optic body 30 separated a distance apart. A plurality of struts 40 extend between the fluid optic body 20 and the second optic body 30 and couple the fluid optic body 20 to the second optic body 30, thereby defining a central space. In certain embodiments, another lens (e.g., as a solid lens) may be disposed in this central space, as discussed in detail below. When the IOL 10 is implanted within the capsular bag of a patient's eye such that the fluid optic body 20 and second optic body 30 are disposed on the optical axis (A) (allowing light traversing the IOL 10 to be refracted by fluid optic body 20 and/or second optic body 30), the compression of the capsular bag during disaccommodation can cause the plurality of struts 40 to deform (e.g., rotate, flex, bend, bow out) in manner that changes the shape of the fluid optic body 20, thereby altering the optical power of the IOL 10.

[0019] The fluid optic body 20 of IOL 10 can have a variety of configurations but generally comprises a sealed cavity for containing an optical fluid, the sealed cavity being at least partially defined by a deformable optical membrane. As best shown in FIG. 2, the fluid optic body 20 comprises a deformable optical membrane 22, a second optical membrane 24, and a circumferential sidewall 26 extending therebetween such that a sealed cavity 28 (which may contain an optical fluid) is formed within the fluid optic body 20. As discussed in detail below, the sidewall 26 can be coupled to the deformable optical membrane 22 such that rotation/flexion of at least a portion of the sidewall 26 (e.g., due to movement of the struts 40) increases tension on the deformable optical membrane 22. In certain embodiments, the second optical membrane 24 may be more rigid than the deformable optical membrane 22 so as to provide a relatively rigid surface upon which the axial force can be applied during compression of the capsular bag. For example, the second optical membrane 24 may be formed from a stiffer (e.g., less elastic) material than deformable optical membrane 22. Alternatively, the second optical membrane 24 may be formed of the same material deformable optical membrane 22 but may have an increased thickness relative to deformable optical membrane 22.

[0020] In certain embodiments, the junction of the second optical membrane 24 and the sidewall 26 can be a relatively-sharp edge (e.g., the surfaces may be substantially perpendicular to one another) so as to create a discontinuous capsular bend at this junction during compression of the capsular bag. Likewise, such a discontinuous bend can be generated at the anterior portion of the IOL 10, for example, via a circumferential lip about the anterior optic body 30.

[0021] The deformable optical membrane 22 i is located anterior to the second optical membrane 24 when disposed within the capsular bag 2 (such that the second optical membrane 24 contacts at least a portion of a posterior surface 6 of the capsular bag 2).

[0022] The second optic body 30 of IOL 10 may include any suitable optic body facilitating the functionality described herein. For example, as depicted in FIGS. 1 -2, second optic body 30 may comprise a solid (i.e., second optic body 30 may lack a cavity). As a result, second optic body 20 may provide a relatively rigid surface upon which the axial force during compression of the capsular bag may be applied. As another example, second optic body 30 may comprise a fluid optic similar to fluid optic body 20. In other words, IOL 10 may comprise both an anterior fluid optic (e.g., second optic body 30) and a posterior fluid optic (e.g., fluid optic body 20) each of which comprises a deformable optical membrane that changes shape upon axial compression of the capsular bag.

[0023] The fluid optic body 20 and the second optic body 30 of IOL 10 may each comprise a variety of materials that include, for example, fluid impermeable and biocompatible materials. In particular, the deformable optical membrane 24 and the second optical membrane 24 may each be constructed of materials that are optically transparent and smooth (e.g., an optical-quality surface). Exemplary materials include, hydrogels, silicones, acrylic materials, and other elastomeric polymers and soft plastics. For example, the silicone materials can be unsaturated terminated siloxanes, such as vinyl terminated siloxanes or multi-vinyl terminated siloxanes. Non-limiting examples include vinyl terminated diphenylsiloxane-dimethylsiloxane copolymers, vinyl terminated polyphenylmethylsiloxanes, vinyl terminated phenylmethylsiloxane-diphenyidimethylsiloxane copolymers, vinyl terminated polydimethylsiloxanes and methacrylate, and acrylate functional siloxanes. In other embodiments the lens-forming materials can be a hydrogel or a hydrophobic acrylic, such as the AcrySof® acrylic. Use of elastic/flexible materials can also enable the IOL 10 or optic body 20 to be folded upon itself during implantation, thereby decreasing the size of the incision required to insert the IOL 10 into the capsular bag 2. The present disclosure contemplates that fluid optic body 20 and the second optic body 30 may be constructed of the same or different materials.

[0024] In certain embodiments, fluid optic body 20, second optic body 30, and struts 40 can comprise a unitary body formed of the same material throughout, though these portions may vary in thickness in order to provide for desired movement of the IOL 10, as otherwise discussed herein. For example, second optic body 30 may be thicker than struts 40 and sidewall 26 such that the second optic body 30 provides structural support to the IOL 10 during axial compression of the capsular bag and efficiently transfers the axial force to the struts 40, the sidewall 26, and ultimately to the deformable optical membrane 22. Likewise, the second optical membrane 24 may be thicker relative to the sidewall 26 and deformable optical membrane 22 such that the second optical membrane 24 may also provide structural support for the IOL 10 upon axial compression of the capsular bag. Additionally, this configuration may allow the sidewall 26 to flex or rotate in response to the deformation of struts 40, thereby tensioning/stretching the deformable optical membrane 22.

[0025] In certain embodiments, various portions of the IOL 10 may be made of materials of different stiffness to provide for desired movement of the IOL 10, as otherwise discussed herein. For example, the deformable optical membrane 22 may be made of an elastomeric material having a low modulus, while the second optical body 30 and second optical membrane 24 may be of a more rigid material.

[0026] The various components of IOL 10 may each have any suitable configuration facilitating accommodation as described herein. For example, fluid optic body 20 and second optic body 30 may each have substantially circular cross sections. Alternatively, fluid optic body 20 and second optic body 30 may each have non-circular cross sections (e.g., oval or elliptical cross-section). Additionally, the sidewall 26 of fluid optic body 20 may have any suitable configuration that facilitates rotation/flexion in response to deformation of the attached struts 40. The sidewall 26 defines a diameter 27 of the fluid optic body 20, and the deformable optical membrane 22 may span that diameter. Upon axial compression of the capsular bag (in the direction indicated by the arrows in FIG. 2), struts 40 impart a force on the sidewall 26, thereby causing deformation of the sidewall 26 in a manner that cause the diameter 27 defined by the sidewall to increase. In particular, the sidewall 26 deforms such that at least a portion of the sidewall 26 rotates about a pivot. This increase in diameter 27 of sidewall 26 may cause a change in the radius of curvature of the deformable optical membrane 22 (e.g., by radially stretching the deformable optical membrane 22).

[0027] The present disclosure contemplates that the term "diameter" may encompass multiple diameters in the case of a fluid optic body 20 having a non-circular cross section (e.g., an elliptical cross section having a transverse and conjugate diameter). Moreover, when the term "diameter" encompasses multiple diameters, deformation of the sidewall in a manner that increases the diameter defined by the sidewall to increase may encompass an increase in one or more of those diameters.

[0028] The optical fluid contained within the cavity 28 of IOL 10 may be any suitable fluid and may include, for example, an incompressible or substantially incompressible fluid exhibiting an index of refraction different that the fluid surrounding the IOL 10. As a result, light passing through the IOL 10 may undergo refraction at both the deformable optical membrane 22 and the second optical membrane 24, the level of refraction being dependent upon the shape of the boundary between the optical fluid and the external fluid (i.e., the shape of the deformable optical membrane 22 and the second optical membrane 24 relative to the optical axis(A)). Exemplary suitable fluids for use in the cavity 28 include fluids with an index of refraction higher than water, for example, an index of refraction greater than 1.3. In certain embodiments, the fluid may exhibit an index of refraction greater than 1.36 or greater than 1.38. In other embodiments, the index of refraction may be in the range of about 1.3 to about 1.8, in the range of about 1.36 to about 1.70, or in the range of about 1.38 to about 1.60. Suitable fluids may include saline, hydrocarbon oils, silicone oils, and silicone gels.

[0029] The optical fluid may be disposed within the cavity 28 during fabrication of the IOL 10, after fabrication but before implantation of the IOL 10, or after implantation of the IOL 10. For example, the optic body 20 may include a fill port that can be sealed or plugged after filling the cavity 28. Additionally or alternatively, the optical fluid may be injected through the optic body 20 and the optic body 20 may be self-sealing.

[0030] The plurality of struts 40 may have any suitable configuration facilitating accommodation of the IOL 10 as described herein. For example, each of the plurality of struts 40 may generally extend between the fluid optic body 20 and the second optic body 30 (thereby coupling the fluid optic body 20 to the second optic body 30) and may be configured to move or deform in response to axial compression of the capsular bag (as described in detail below). In particular, as shown in FIG. 1, each of the plurality of struts 40 may extend in a direction substantially parallel to the optical axis (A) and couple a point or region on the circumference of the fluid optic body 20 to a point or region on the circumference of the second optic body 30. Although a particular number of struts 40 are depicted, the present disclosure contemplates any suitable number of struts 40 facilitating to translation of axial compression of the capsular bag into modification of the curvature of at least the deformable optical membrane 22.

[0031] In certain embodiments, each of the struts 40 may be curved. As a result, the axial force imparted by the capsular bag may tend to increase radial bowing of the struts 40. As a result, the maximum diameter of the IOL 10 in the disaccommodated state may be increased.

[0032] In certain embodiments, struts 40 may have cross-sectional areas that varies with length so as to provide additional support and/or to provide for the movement of the struts 40 as discussed herein. For example, portions of a struts 40 that are closer to the fluid optic body 20 (e.g., the posterior end of the strut 40) may be thinner relative to the portions of the strut 40 closer to the second optic body 30 (e.g., the anterior end of the strut). As a result, the posterior end of the strut 40 may move in response to axial compression so as to increase the deformation of the deformable optical membrane 22.

[0033] In certain embodiments, adjacent struts 40 may be coupled to one another via a ring-like structure 46 disposed around the circumference of the IOL 10. Ring 46 may increase stability of the IOL 10 within the capsular bag and/or improve the uniformity of the force exerted on the struts 40 and deformable membrane 22 as the IOL 10 is axially compressed. Additionally, the axial force exerted on the second optic body 30 may be more evenly distributed between the struts 40 due to their coupling with the ring 46, and the ring 46 may provide additional support to the struts 40 at a location between the fluid optic body 20 and the second optic body 30 in which stress on the struts 40 during axial compression is concentrated.

[0034] In certain embodiments, the fluid optic body 20, the second optic body 30, and the struts 40 may each be dimensioned such that, in its resting state (as shown in FIG. 2), the IOL 10 may have a length along the optical axis (A) that is slightly larger than the anterior-to-posterior depth of the capsular bag. As a result, tension exerted by the capsular bag on the IOL 10 upon implantation may substantially maintain the IOL 10 in a desired position. Additionally, the fluid optic body 20, the second optic body 30, and the struts 40 may each be dimensioned such that the surface area that engages the anterior and posterior surfaces of the capsular bag is maximized while minimizing the overall volume of the IOL 10. For example, the radial dimensions of the IOL 10 may be slightly smaller than diameter of the capsular bag to help maximize the transfer of energy to the IOL 10 by minimizing loss of energy due to lateral stretching of the IOL 10.

[0035] Movement of the exemplary IOL 10 will now be described as the capsular bag 2 goes from an accommodated state, as shown in FIG. 3A, to a disaccommodated state, as shown in FIG. 3B. With reference first to FIG. 3A, the IOL 10 and capsular bag 2 are depicted in their accommodated state during which the ciliary muscles are contracted such that zonules extending between the ciliary muscles and the capsular bag 2 are slack. As a result, there exists little radial tension on the capsular bag 2. As discussed above, IOL 10 may be sized such that, in this state, the fluid optic body 20 and the second optic body 30 may each be in contact with the capsular bag 2, but the capsular bag 2 may exert a minimum amount of axial force on the IOL 10. This minimum amount of axial force may help maintain the IOL 10 in a desired position within the capsular bag 2.

[0036] Upon relaxation of the ciliary muscles, the zonules will exert radial tension on the capsular bag 2 (as indicated by the solid arrows in FIG. 3B), which causes axial compression of the capsular bag 2 (as indicated by the broken arrows). As a result, the capsular bag 2 may exert a force on the IOL 10 (specifically fluid optic body 20 and second optic body 30), and this force may cause a decrease in the separation distance between fluid optic body 20 and second optic body 30. This decrease in the separation distance between fluid optic body 20 and second optic body 30 may contribute to the optical power change of the IOL 10. However, the primary factor affecting the optical power change of the IOL 10 may be the curvature change of the deformable optic membrane 22 resulting from deformation of struts 40, as discussed further below.

[0037] As is illustrated by comparing FIGS. 3A and 3B, the maximum diameter of IOL 10 (e.g., the diameter measured at the ring 46) may increase due deformation of struts 40 resulting from axial compression of the capsular bag 2. In particular, the posterior-curved portions of the struts 40 located adjacent to fluid optic body 20 may move radially and/or posteriorly (e.g., through rotation about the fluid optic body 20). Because the posterior-most ends of struts 40 are coupled to the sidewall 26, such deformation of the struts 40 may impart a force upon the sidewall 26 and cause deformation of the sidewall 26. For example, at least a portion of the sidewall 26 may rotate outward about a pivot such that the diameter 27 defined by the sidewall 26 increases. In certain embodiments, the portion of sidewall 26 defining diameter 27 (i.e., the point at which sidewall 26 and deformable optical membrane 22 intersect) may anteriorly raise the periphery of the deformable optic membrane 22. Deformation of sidewall 26 in a manner that increases diameter 27 may increase tension and radial stretching of the deformable membrane 22. As a result, the deformable optical membrane 22 may exhibit a flatter profile (e.g., a larger radius of curvature). Additionally, the distance between the deformable optical membrane 22 and the second optical membrane 24 (along the optical axis (A)) may be decreased. As the radial force on the capsular bag 2 is relaxed, the capsular bag 2 and IOL 10 may return to their biased configuration shown in FIG. 2.

[0038] With reference now to FIGS. 4A and 4B, finite element analysis of exemplary simulated movement of the IOL 10 is depicted as the IOL 10 moves from its resting or accommodated state (as shown in phantom outline) to its disaccommodated state (as shown in solid color). Upon axial compression of the capsular bag, the axial compressive force on the IOL 10 increases, initiating movement of the struts 40 and deformation of the sidewall 26. This movement of struts 40 transfers at least a portion of the force exerted on IOL10 to the sidewall 26, which in turn transfers at least a portion of that force to deformable optical membrane 22. The resulting stress on deformable optical membrane 22 is at a maximum along the optical axis as the deformable optical membrane 22 is pulled from all sides. As compression continues, the struts 40 rotate further and the cavity 28 containing the optical fluid changes shape as the deformable optical membrane 22 becomes flatter.

[0039] As the thickness of the sidewall 26 increases and/or its height decreases, the overall power change of the IOL 10 during compression may decrease or a greater axial compressive force to achieve the same deformation may be required. In order to achieve maximum power change, the thickness of the sidewall 26 (i.e., in a radial direction) may be significantly less than its height (i.e., along the optical axis (A)). Additionally, increased thickness of the junction of the deformable optical membrane 22 and the sidewall 26 may help in distributing the deformation from the struts 40 more uniformly on the optic membrane 22, which may reduce the number of struts 40 needed without inducing optical aberrations in the deformable optical membrane 22.

[0040] The present disclosure contemplates that the thickness of the deformable optical membrane 22 may be manipulated (e.g., increased, decreased, and/or varied about its area) so as to maintain good visual acuity and high power change throughout accommodation. For example, a convex deformable optical membrane 22 (i.e., a membrane in which the central portion is thicker than the periphery) with a low power may reduce aberrations during accommodation. Alternatively, if the deformable optical membrane 22 is flat (i.e., the membrane exhibits a substantially constant thickness), it will deform more easily in the central part than the periphery. Additionally, the present disclosure contemplates that each surface of the IOL 10 within the optical aperture lens can be spherical or aspheric so as to alter the optical properties of light traversing therethrough. For example, the various surfaces of the second optic body 30 provide various locations to include complex optical designs, in accordance with that process as known in the art and modified in accordance with the present teachings.

[0041] The above-described IOL 10 may be fabricated using any suitable techniques known in the art and modified in light of the present teachings. For example, IOL 10 may be injection molded such that the struts 40 and deformable optical membrane 22 can be biased to the position shown in FIG. 2. That is, in the absence of substantial external forces (e.g., in its free form outside the eye), the IOL 10 can be configured to maintain a radius of curvature approximate its shape in an accommodated state. Accordingly, the struts 40 would tend to return to this biased position upon removal of or relaxation of the axial compressive force (e.g., as the capsular bag goes from its disaccommodated configuration to its accommodated configuration). This biased configuration may especially aid those patients in which the ciliary bodies have lost some of their contractility or the capsular bag 2 has lost some of its elasticity, for example, due to age.

[0042] With reference now to FIG. 5, another exemplary IOL 510 is depicted. The IOL 510 is substantially similar to the IOL 10 depicted in FIG. 1 in that it includes a fluid optic body 520, a second optic body 530, and a plurality of struts 540 extending therebetween. Similarly, the fluid optic body 520 defines a cavity 528 for containing a fluid and is configured to change shape upon axial compression of the IOL 510 due to movement of the struts 540. The IOL 510 differs, however, in that adjacent struts 540 are not coupled to one another at a location between fluid optic bodies 520 and second optic body 530 (e.g., via a ring 46 as shown in FIG. 1). Although the ring 46 can provide stability in some aspects, a lens such as IOL 510 lacking such a ring may ease implantation (e.g., by allowing the IOL 510 to be folded into a more compact shape) and may ease viscoelastic removal. In certain embodiments, the dimensions of IOL 510 may be have a greater overall diameter relative to IOL 10 so as to extend more radially within the capsular bag, thereby increasing stability of the IOL 510 (e.g., by reducing rotation) following implantation.

[0043] With reference now to FIG. 6, finite element analysis of exemplary simulated movement of the IOL 510 is depicted as the lens 510 moves from its resting or accommodated state (as shown in phantom outline) to its disaccommodated state (as shown in solid color). Upon axial compression of the capsular bag, the axial compressive force on the IOL 510 initiates movement of the second optic body 530 and thus rotation and/or bowing out of struts 540. This rotation results in a radial force applied to the deformable optical membrane 522 such that the cavity 528 containing the optical fluid changes shape, thereby altering the power of the fluid optic body 520.

[0044] With reference now to FIG. 7, an exemplary simulation depicts the optical power change of the exemplary IOL 510 as it moves from its accommodated state to its disaccommodated state. As the lens 510 is compressed from its accommodated state (compression = 0 mm) to its disaccommodated state (compression = 0.5 mm), the IOL 510 exhibits an optical power change of -7 diopter, which is a decrease in the focusing power (for far vision as the light rays from far objects are more parallel relative to those from near objects).

[0045] With reference now to FIG. 8, a simulated modulation transfer function (MTF) and power change is depicted for a lens in accordance with FIG. 5. The simulation was performed with a 3mm pupil and a model eye. In the simulation, a simple spherical convex type membrane is used. Since dynamic aberrations are reasonably compensated by the membrane, all MTF curves are close to the diffraction limited MTF over ∼8D power change.

[0046] With reference now to FIG. 9, another exemplary IOL 910 is depicted. IOL 910 may be substantially similar to IOL 510 depicted of FIG. 5, but differing in that the IOL 910 additionally includes a mechanical block 950 configured to limit relative axial movement of fluid optic body 920 and second optic body 930. In certain embodiments, mechanical block 950 comprises a ring structure disposed around the optical axis between the second optic body 930 and the fluid optic body 920 such that the ring structure constrains or interferes with axial movement of the second optic body 930 toward the fluid optic 920 after a selected amount of deformation. In certain embodiments, mechanical block 950 may be supported by a second plurality of struts 952 which extend from the fluid optic body 920 at locations between the plurality of struts 940 supporting the second optic body 930. The second plurality of struts 952 may provide increased resistance to compressive force as compared to struts 940 (e.g., by using a stiffer/less-flexible material or by having an increased thickness). Thus, when the second optic body 930 is compressed against the mechanical block 950, further compression of the IOL 910 is resisted, thereby preventing further rotation of the struts 940, and ultimately, further deformation of the deformable membrane 922.

[0047] FIG. 10 depicts another exemplary embodiment of an IOL 1010 that includes a mechanical block 1050 differing from that of FIG. 9 in that it physically interferes with the rotation of the struts 1040. For example, as shown in FIG. 10, the fluid optic body 1020 includes a second sidewall 1050 that extends radially beyond the sidewall 1026 such that the posterior portion of the struts 1040 contacts the second sidewall 1050 after a certain level of axial compression. Thus, when the struts 1040 are compressed against the mechanical block 1050, further movement of the struts 1040 is constrained, thereby preventing further deformation of the deformable membrane 1022, as discussed in detail above.

[0048] Alternatively or additionally, deformation of the deformable membrane may be controlled by limiting the movement of the deformable membrane directly. For example, with reference not to FIG. 11, another exemplary IOL 1110 having a mechanical block 11150 is depicted. Mechanical block 1150 may interfere with the curvature change that can be exhibited by the deformable optical membrane 1122. The second optical membrane 1124 of IOL 1110 may differ from the second optical membrane 24 of IOL 10 (described with respect to FIG. 1) in that the second optical membrane 1124 may comprise a solid portion extending towards the deformable optical membrane 1122 (i.e., within the cavity 1128). As such, the movement of the deformable optical membrane 1122 can be constrained from moving beyond the surface profile of the mechanical block. Although the mechanical block 1150 is shown as being planar, the present disclosure contemplates that the mechanical block 1150 may have any suitable shape (e.g., mechanical block 1150 may be convex to limit the deformation of the membrane 1122, depending on the desired optical power change).

[0049] In addition to the structural stability noted above, the mechanical blocks described herein may also provide a consistent, maximum change at various levels of compression and/or prevent refractive errors that typically occur at higher levels of power change. With reference to the graph depicted in FIG. 12, for example, though the IOLs described herein may be subject to additional compressive force, the power change of the IOL may nonetheless remain substantially constant as the mechanical blocks can provide an equivalent resistive force that prevents further compression of the IOLs. Although such action may limit the maximum power change that can be achieved (as shown in the dotted line of FIG. 12), the mechanical blocks can advantageously provide a consistent maximum deformation. Moreover, failure or aberrations (e.g., high refractive errors) that can result, for example, by over-tensioning the deformable optical membranes, can be avoided by limiting the maximum allowable deformation of the deformable optical membrane.

[0050] As noted above, the IOLs described herein generally provide a space between the optic bodies and struts within which a solid lens can be disposed. Whereas the curvature of the deformable optical membrane (e.g., deformable optical membrane 22 of FIG. 1) is generally responsible for the optical power of the IOL, a solid lens disposed within the space can additionally provide for power change or other features (e.g., spherical, aspheric, toric features), as is known in the art. To further aid delivery, the solid lens can also be elastomeric or foldable to ease insertion into the capsular bag. Additionally or alternatively, a second optic body of the IOLs described herein can provide for such spherical, aspherical, or toric features, as noted above.

[0051] In use, the exemplary accommodative intraocular lenses described herein are adapted to be inserted in the human eye using conventional surgical techniques modified in accordance with the present teachings. Typically, the natural crystalline lens is first removed and the IOL can be folded into a compact size for insertion through an incision or opening in the capsular bag. Following insertion, a single piece IOL (e.g., IOL 10) can be manipulated to assume its proper position in the capsular bag, as described above. Alternatively, an IOL in which multiple components are delivered to the capsular bag independently can be assembled in situ (e.g., by coupling the struts 40 to a fluid optic body 20 delivered independently). In some aspects, the IOLs described herein can be implanted in the capsular bag without optical fluid contained within the cavity of the fluid optic body such that the method for implantation can further include filling the cavity with the optical fluid while the lens is disposed within the eye (e.g., via injection). In this manner, implantation of the exemplary IOLs described herein can aid in restoring natural vision by providing an accommodative, curvature-changing refractive lens that mimics how the natural crystalline lens changes shape in response to movement of the ciliary bodies to variously bend incoming light onto the retina depending on the desired focal point.

[0052] The term intraocular lens or "IOL" is used herein to refer to any lens or lens component adapted to be inserted into a patient's eye. Such a lens can be phakic or aphakic (also referred to in the art as pseudophakic) to restore, improve, or partially correct vision. Phakic lenses are used in conjunction with the natural lens of an eye to correct refractive errors such as myopia (near-sightedness), hyperopia (far-sightedness) and astigmatism, coma or other higher order refractive errors (blurred vision due to poor light focusing on the retina due to an irregularly shaped cornea or, in some instances, an irregularly shaped natural lens). An aphakic or pseudophakic lens is inserted in the eye subsequent to removal of the natural lens due to disease, e.g., a cataract or clouding of the natural lens. The aphakic or pseudophakic lens can also restore, improve, or partially correct vision by providing a power comparable to that of the natural lens and can also correct myopia, hyperopia or other refractive errors. Either type of lens may be implanted in the anterior chamber in front of the iris or in the posterior chamber behind the iris and in front of the natural lens or in the region where the natural lens was before removal.

Claims

1. An intraocular lens (10) configured to be implanted within a capsular bag of a patient's eye, the lens comprising:
a fluid optic body (20) comprising a cavity (28) for containing an optical fluid, the cavity defined by:

a deformable optical membrane (22) configured to extend across an optical axis of a patient's eye, the deformable optical membrane (22) defining an anterior surface of the cavity;

a second optical membrane (24) configured to extend across the optical axis of the patient's eye, the second optical membrane defining a posterior surface of the cavity; and

a sidewall (26) having an anterior end connected to the deformable optical membrane and a posterior end connected to the second optical membrane such that the sidewall extends between the deformable optical membrane (22) and the second optical membrane (24); and

a second optic body (30) spaced a distance apart from the fluid optic body (20) and configured to extend across the optical axis of the patient's eye; and

a plurality of struts (40) extending from the sidewall and coupling the fluid optic body (20) to the second optic body (30),

wherein the struts (40) are configured such that axial compression of the capsular bag along the optical axis (A) causes the plurality of struts to rotate the sidewall about a pivot in a manner that increases a diameter of the cavity at the anterior end of the sidewall relative to a diameter of the cavity at the posterior end of the sidewall such that a radius of curvature of the deformable optical membrane (22) is increased.

2. The intraocular lens of claim 1, the fluid optic body (20) and the second optic body (30) each being disposed on the optical axis wherein the fluid optic body is configured to be in contact with a first surface of the capsular bag and the second optical body is configured to be in contact with a second surface of the capsular bag when the intraocular lens is implanted into the capsular bag of a patient's eye.

3. The intraocular lens of claim 1, the deformable optical membrane having a tension and wherein the sidewall and the deformable optical membrane are configured such that tension on the deformable optical membrane is increased upon the rotation of the sidewall (26) in the manner that increases in the diameter of the cavity.

4. The intraocular lens of claim 1, wherein the deformable optical membrane (22) is configured stretch radially upon the rotation of the sidewall (26) in the manner that increases in the diameter of the cavity.

5. The intraocular lens of claim 1, wherein the struts (40) are configured such that the axial compression of the capsular bag causes deformation of the struts (40).

6. The intraocular lens of claim 5, wherein each of the struts is curved, and configured such that the axial compression of the capsular bag increases radial bowing of the struts (40) outward relative to the optical axis of the patient's eye.

7. The intraocular lens of claim 6, each of the struts (40) having a radius of curvature wherein the struts are configured such that the radius of curvature of each of the struts decreases in response to deformation of the struts.

8. The intraocular lens of claim 1, configured such that the distance between the fluid optic body (20) and the second optic body (30) along the optical axis decreases upon axial compression of the capsular bag.

9. The intraocular lens of claim 1, wherein each of the plurality of struts (40) comprises a curved portion that is concave relative to the optical axis.

10. The intraocular lens of claim 1, wherein the second optic body (30) comprises a solid optic.

11. The intraocular lens of claim 1, wherein each of the plurality of struts are coupled to one another via a circumferential ring disposed between the fluid optic body and the second optic body.

12. The intraocular lens of claim 11, the circumferential ring having a diameter and wherein the struts and the circumferential ring are configured such that the diameter of the circumferential ring increases upon the axial compression of the capsular bag.

Ansprüche

1. Intraokularlinse (10), die zur Implantation in einen Kapselsack eines Auges eines Patienten ausgelegt ist, wobei die Linse das Folgende umfasst:

einen Fluid-Optikkörper (20), umfassend einen Hohlraum (28) zum Enthalten eines optischen Fluids, wobei der Hohlraum definiert wird durch:

eine verformbare optische Membran (22), die dazu ausgelegt ist, sich über eine optische Achse eines Auges eines Patienten zu erstrecken, wobei die verformbare optische Membran (22) eine Vorderseite des Hohlraums definiert;

eine zweite optische Membran (24), die dazu ausgelegt ist, sich über die optische Achse des Auges des Patienten zu erstrecken, wobei die zweite optische Membran eine Rückseite des Hohlraums definiert; und

eine Seitenwand (26) mit einem vorderen Ende, das mit der verformbaren optischen Membran verbunden ist, und einem hinteren Ende, das mit der zweiten optischen Membran verbunden ist, so dass sich die Seitenwand zwischen der verformbaren optischen Membran (22) und der zweiten optischen Membran (24) erstreckt; und

einen zweiten Optikkörper (30), der im Abstand vom Fluid-Optikkörper (20) angeordnet ist und dazu ausgelegt ist, sich über die optische Achse des Auges des Patienten zu erstrecken; und

eine Vielzahl von Streben (40), die sich von der Seitenwand erstrecken und den Fluid-Optikkörper (20) mit dem zweiten Optikkörper (30) verbinden,

wobei die Streben (40) so ausgelegt sind, dass eine axiale Kompression des Kapselsacks entlang der optischen Achse (A) verursacht, dass die Vielzahl von Streben die Seitenwand um einen Drehpunkt drehen, derart, dass ein Durchmesser des Hohlraums am vorderen Ende der Seitenwand im Verhältnis zu einem Durchmesser des Hohlraums am hinteren Ende der Seitenwand vergrößert wird, so dass ein Krümmungsradius der verformbaren optischen Membran (22) vergrößert wird.

2. Intraokularlinse nach Anspruch 1, wobei der Fluid-Optikkörper (20) und der zweite Optikkörper (30) jeweils auf der optischen Achse angeordnet sind, wobei der Fluid-Optikkörper dazu ausgelegt ist, mit einer ersten Oberfläche des Kapselsacks in Kontakt zu stehen, und der zweite Optikkörper dazu ausgelegt ist, mit einer zweiten Oberfläche des Kapselsacks in Kontakt zu stehen, wenn die Intraokularlinse in den Kapselsack eines Auges eines Patienten implantiert wird.

3. Intraokularlinse nach Anspruch 1, wobei die verformbare optische Membran eine Spannung aufweist und wobei die Seitenwand und die verformbare optische Membran so ausgelegt sind, dass die Spannung auf der verformbaren optischen Membran erhöht wird, wenn die Seitenwand (26) so gedreht wird, dass der Durchmesser des Hohlraums zunimmt.

4. Intraokularlinse nach Anspruch 1, wobei die verformbare optische Membran (22) dazu ausgelegt ist, sich radial zu dehnen, wenn die Seitenwand (26) so gedreht wird, dass der Durchmesser des Hohlraums zunimmt.

5. Intraokularlinse nach Anspruch 1, wobei die Streben (40) so ausgelegt sind, dass die axiale Kompression des Kapselsacks eine Verformung der Streben (40) verursacht.

6. Intraokularlinse nach Anspruch 5, wobei jede der Streben gebogen ist, und so ausgelegt ist, dass die axiale Kompression des Kapselsacks eine radiale Biegung der Streben (40) nach außen bezüglich der optischen Achse des Auges des Patienten erhöht.

7. Intraokularlinse nach Anspruch 6, wobei jede der Streben (40) einen Krümmungsradius aufweist, wobei die Streben so ausgelegt sind, dass der Krümmungsradius jeder der Streben als Reaktion auf eine Verformung der Streben abnimmt.

8. Intraokularlinse nach Anspruch 1, die so ausgelegt ist, dass der Abstand zwischen dem Fluid-Optikkörper (20) und dem zweiten Optikkörper (30) entlang der optischen Achse bei axialer Kompression des Kapselsacks abnimmt.

9. Intraokularlinse nach Anspruch 1, wobei jede der Vielzahl von Streben (40) einen gebogenen Abschnitt umfasst, der bezüglich der optischen Achse konkav ist.

10. Intraokularlinse nach Anspruch 1, wobei der zweite Optikkörper (30) eine feste Optik umfasst.

11. Intraokularlinse nach Anspruch 1, wobei die Vielzahl von Streben über einen Umfangsring, der zwischen dem Fluid-Optikkörper und dem zweiten Optikkörper angeordnet ist, jeweils miteinander verbunden sind.

12. Intraokularlinse nach Anspruch 11, wobei der Umfangsring einen Durchmesser aufweist und wobei die Streben und der Umfangsring so ausgelegt sind, dass der Durchmesser des Umfangsrings bei axialer Kompression des Kapselsacks zunimmt.

Revendications

1. Lentille intraoculaire (10) conçue pour être implantée dans un sac capsulaire d'un œil d'un patient, la lentille comprenant :
un corps optique à fluide (20) comprenant une cavité (28) pour contenir un fluide optique, la cavité étant définie par :

une membrane optique déformable (22) conçue pour s'étendre en travers d'un axe optique d'un œil d'un patient, la membrane optique déformable (22) définissant une surface antérieure de la cavité ;

une seconde membrane optique (24) conçue pour s'étendre en travers de l'axe optique de l'œil du patient, la seconde membrane optique définissant une surface postérieure de la cavité ; et

une paroi latérale (26) possédant une extrémité antérieure reliée à la membrane optique déformable et une extrémité postérieure reliée à la seconde membrane optique de sorte que la paroi latérale s'étende entre la membrane optique déformable (22) et la seconde membrane optique (24) ; et

un second corps optique (30) espacé, sur une certaine distance, du corps optique à fluide (20) et conçu pour s'étendre en travers de l'axe optique de l'œil du patient ; et

une pluralité d'entretoises (40) s'étendant depuis la paroi latérale et reliant le corps optique à fluide (20) au second corps optique (30),

dans laquelle les entretoises (40) sont conçues de sorte qu'une compression axiale du sac capsulaire le long de l'axe optique (A) amène la pluralité d'entretoises à faire tourner la paroi latérale autour d'un pivot d'une manière qui augmente un diamètre de la cavité au niveau de l'extrémité antérieure de la paroi latérale par rapport à un diamètre de la cavité au niveau de l'extrémité postérieure de la paroi latérale de sorte qu'un rayon de courbure de la membrane optique déformable (22) soit augmenté.

2. Lentille intraoculaire selon la revendication 1, le corps optique à fluide (20) et le second corps optique (30) étant chacun disposés sur l'axe optique, dans laquelle le corps optique à fluide est conçu pour être en contact avec une première surface du sac capsulaire et le second corps optique fluide est conçu pour être en contact avec une seconde surface du sac capsulaire lorsque la lentille intraoculaire est implantée dans le sac capsulaire d'un œil d'un patient.

3. Lentille intraoculaire selon la revendication 1, la membrane optique déformable ayant une tension et dans laquelle la paroi latérale et la membrane optique déformable sont conçues de sorte qu'une tension sur la membrane optique déformable soit augmentée lors de la rotation de la paroi latérale (26) de la manière qui augmente dans le diamètre de la cavité.

4. Lentille intraoculaire selon la revendication 1, dans laquelle la membrane optique déformable (22) est conçue pour s'étirer radialement lors de la rotation de la paroi latérale (26) de la manière qui augmente dans le diamètre de la cavité.

5. Lentille intraoculaire selon la revendication 1, dans laquelle les entretoises (40) sont conçues de sorte que la compression axiale du sac capsulaire provoque la déformation des entretoises (40).

6. Lentille intraoculaire selon la revendication 5, dans laquelle chacune des entretoises est incurvée, et conçue de sorte que la compression axiale du sac capsulaire augmente une cambrure radiale des entretoises (40) vers l'extérieur par rapport à l'axe optique de l'œil du patient.

7. Lentille intraoculaire selon la revendication 6, chacune des entretoises (40) ayant un rayon de courbure, dans laquelle les entretoises sont conçues de sorte que le rayon de courbure de chacune des entretoises diminue en réponse à une déformation des entretoises.

8. Lentille intraoculaire selon la revendication 1, conçue de sorte que la distance entre le corps optique à fluide (20) et le second corps optique (30) le long de l'axe optique diminue lors d'une compression axiale du sac capsulaire.

9. Lentille intraoculaire selon la revendication 1, dans laquelle chaque entretoise de la pluralité d'entretoises (40) comprend une partie incurvée qui est concave par rapport à l'axe optique.

10. Lentille intraoculaire selon la revendication 1, dans laquelle le second corps optique (30) comprend une optique pleine.

11. Lentille intraoculaire selon la revendication 1, dans laquelle chaque entretoise de la pluralité d'entretoises est reliée à une autre par l'intermédiaire d'un anneau circonférentiel disposé entre le corps optique à fluide et le second corps optique.

12. Lentille intraoculaire selon la revendication 11, l'anneau circonférentiel ayant un diamètre, et dans laquelle les entretoises et l'anneau circonférentiel sont conçus de sorte que le diamètre de l'anneau circonférentiel augmente lors de la compression axiale du sac capsulaire.

Drawing